Supported Palladium Catalyzed Carbonylative Coupling Reactions using Carbon Monoxide as C1 Source

被引:17
|
作者
Shaifali [1 ,2 ]
Sheetal [1 ,2 ]
Das, Pralay [1 ,2 ]
机构
[1] CSIR Inst Himalayan Bioresource Technol, Chem Technol Div, Palampur 176061, HP, India
[2] Acad Sci & Innovat Res AcSIR, Ghaziabad 201002, India
来源
CHEMICAL RECORD | 2022年 / 22卷 / 01期
关键词
CO; CO sources; Heterocycles synthesis; Recyclability; Supported palladium catalysts; EFFICIENT HETEROGENEOUS CATALYST; ONE-STEP SYNTHESIS; ARYL IODIDES; PHOSPHINE-FREE; OXIDATIVE CARBONYLATION; ARYLBORONIC ACIDS; REUSABLE CATALYST; FREE AMINOCARBONYLATION; N-FORMYLSACCHARIN; ON-CARBON;
D O I
10.1002/tcr.202100157
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The carbonylative reactions of aryl halides, boronic acids, amines, activated alkene and alkynes under CO and supported palladium catalyzed conditions are very popular reactions for the synthesis of bioactive molecules, pharmaceuticals, polymers, peptides, intermediates and fine chemicals synthesis. Due to cost effectiveness and easy handling of recyclable supported palladium catalyst, it became more popular among researchers either working in academic institute or industry. In recent years, irrespective of poisoning effect of CO with palladium as major limitation, several advancements have been done through surface selection, designing and condition improvement to achieve high yield in the area of carbonylative coupling reactions. We hope this review will be helpful as a ready reference of last 20 years in the field of CO insertion reactions using diverse range of supported palladium catalysts under carbon monoxide or its sources as C1 source.
引用
收藏
页数:22
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